TEAM KERGIDES was made for THE GREAT STRIDES walk for CF. On that day alone we raised $4800 for the foundation and had over 150 ppl wore the logo of TEAM KERGIDES. Plus, we raised another $500+ in shows we held called "find a cure" shows. Those events had bands play and raise money for the causee. Now to the internet. We created this myspace to further extend our members,hopefully you our friends will help with the cause. we have the power if you have even the slightest bit of ambition, the tiniest flame and you fan it rigt it will ablaze, and with that
you can do anything, anything you want. You can even fix Cystic Fibrosis. We plan on getting many styles of t-shirts made an soon in the near future they will be avialable. We are hoping this will become a flurishing clothing line that will give the money to the CF foundation......... so when the soldiers of cf ask your help help them...
"Be an Angel"This is a site for all those suited for the purpouse. This site is an awarness site about a life-threatening genetic disease affecting approximately 30,000 people in the United States. We must be the army, and the angels for this cause. Everyone and anyone is welcome. I shout my message to you.For people with the disease, a defective gene causes the body to produce a faulty protein that leads to abnormally thick, sticky mucus that clogs the lungs and can result in fatal lung infections. The mucus also obstructs the pancreas, causing difficulty for a person to absorb nutrients in food and can block the bile duct in the liver, eventually causing permanent damage in approximately six percent of people with CF.In addition, more than 10 million Americans are genetic carriers. Carriers each have one copy of the defective CF gene, but do not have the disease and its symptoms. It takes two copies of the gene -- one from each parent -- for a child to be born with cystic fibrosis. Each time two carriers conceive, there is a 25 percent chance that their child will have CF; a 50 percent chance that the child will be a carrier of the CF gene but not have the disease; and a 25 percent chance that the child will not be a carrier and not have the disease.There is no cure yet. But lets fix something together!
IF YOU WANT TO BE THE ANGEL JOIN NOW!If you have Cystic Fibrosis--- JOIN TEAM KERGIDES this is for you!!!! and any one that is a ANGEL
MORE INFO GO TOOO...... http://www.cff.org/home/http://www.cff.org/Great_Strides/dsp
_DonationPage.cfm?walkid=4453&idUser=179984 GO THERE TO DONATE TO US!!!!!!!!!!!!!!!
Be An Angel. Help spread the word.
Copy the code below and paste onto your myspace.
BECOME A CURE FINDER!!!
http://www.cff.org/ways_to_give/become_a_cure_finder/
MAKE A DONATION!!!
http://www.cff.org/ways_to_give/make_a_donation/
